Deimann W, Freeman R, Fahimi H D
J Histochem Cytochem. 1981 May;29(5):678-81. doi: 10.1177/29.5.7252131.
A scanning transmission electron microscope (STEM) was used to examine ultrathin sections of rabbit white skeletal muscle. Lactic dehydrogenase (LDH) activity was localized in the tissue using the tetra-nitro blue tetrazolium (TNBT) method. For most specimens postfixation was omitted in order to avoid reoxidation and solubilization of the formazan by osmium tetroxide. The STEM image revealed sufficient contrast of the intracellular structures and apparently electron-dense reaction product in the sarcoplasmic reticulum and mitochondria. Substantially less contrast was obtained when the same areas were observed by conventional transmission electron microscopy (CTEM). In material postfixed with osmium tetroxide, although the tissue contrast was improved, the TNBT reaction product was focally leached out, exhibiting lower contrast than in unosmicated sections. These results indicate that the fine structural visualization of dehydrogenases with TNBT, the STEM technique as used in the present study is superior to that obtained by CTEM.
使用扫描透射电子显微镜(STEM)检查兔白色骨骼肌的超薄切片。采用四硝基蓝四唑(TNBT)法将乳酸脱氢酶(LDH)活性定位在组织中。对于大多数标本,省略了后固定步骤,以避免四氧化锇使甲臜重新氧化和溶解。STEM图像显示细胞内结构有足够的对比度,并且在肌浆网和线粒体中有明显的电子致密反应产物。当用传统透射电子显微镜(CTEM)观察相同区域时,获得的对比度明显较低。在用四氧化锇后固定的材料中,尽管组织对比度有所提高,但TNBT反应产物局部被浸出,其对比度低于未用锇处理的切片。这些结果表明,就用TNBT对脱氢酶进行精细结构可视化而言,本研究中使用的STEM技术优于CTEM所获得的结果。